Beijing Beishute Maternity & Child Articles Co., Ltd.

FDA Device Registration & Listing · BEIJING, CN · Registration 3006400113

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3006400113
FEI Number
3006400113
Entity Name
Beijing Beishute Maternity & Child Articles Co., Ltd.
City/State/Country
BEIJING, CN
Establishment Address
No. 3 Yuanguang Street, Miyun District, BEIJING 101500, CN
Establishment Type(s)
Foreign Private Label Distributor,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Beijing Beishute Maternity & Child Articles Co., Ltd. (Owner Number: 9096839)
Owner / Operator Contact Address
No. 3 Yuanguang Street, Miyun District, BEIJING, CN-BJ 101500, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Cover

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FXP Cover, Shoe, Operating-Room General, Plastic Surgery Class 1 878.4040 2017-05-22
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 2011-01-14
NRC Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile Obstetrics/Gynecology Class 1 884.5425 2025-05-16
KME Bedding, Disposable, Medical General Hospital Class 1 880.6060 2007-01-19
QKR Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua Unknown Class N N/A 2020-04-03

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Beijing Beishute Maternity & Child Articles Co., Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K823241 Kimberly-Clark Corp. NEW FREEDOM THIN UNSCENTED MAXI PADS 1982-12-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006400113. Last updated year: 2026. Please use registration number 3006400113 when referencing this establishment in official correspondence.
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